A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8654



Internal ID15499880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45876167..45915679hg38UCSC Ensembl
Outerchr10:51680147..51727182hg19UCSC Ensembl
Outerchr10:51350153..51397188hg18UCSC Ensembl
Outerchr10:51350153..51397188hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3839513
hg1947036
hg1847036
hg1747036
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18926, nssv22729, nssv19547
SamplesNA18860, NA18563, NA19007
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv8654
Frequency
Sample Size31
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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